Drugplain

NDC 68071-3362-0

IBUPROFEN 800 mg/1

IBUPROFEN · TABLET, FILM COATED

No Recall History

IBUPROFEN is a tablet, film coated containing ibuprofen at a strength of 800 mg/1. Manufactured by NuCare Pharmaceuticals,Inc..

Key Facts

Brand Name
IBUPROFEN
Generic Name
IBUPROFEN
NDC Code (Package)
68071-3362-0
NDC Code (Product)
68071-3362
Manufacturer
NuCare Pharmaceuticals,Inc.
Strength
800 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Marketing Status
Application #
ANDA090796
Drug Class
Nonsteroidal Anti-inflammatory Drug [EPC]
Marketing Start
12/30/2015

Recall History

No Recall History

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Not medical advice. This information is for reference only. Always consult your doctor or pharmacist.